The Bruyere Brigade

This is the 4th annual walk to end Scleroderma here in Montana. Each year, the support seems to grow, and our family cannot be more grateful for everyone's support. 

The walk is a family friendly, laid-back event that is taking place at Ironwood Park in Billings at 10am on Saturday, September 12th. Even if you do not feel like donating, we would love to see you at the walk to support this great cause. 

Scleroderma is a rare autoimmune disease that generally affects women and symptoms can be very different from patient to patient. 

Raelynn has experienced symptoms since she was 12 years old, which is quite unusual at such a young age. She was officially diagnosed with Diffuse Scleroderma when she was 19. Dealing with this terrible disease is easier knowing that there are friends and family supporting her in this cause. 

Your donation makes a real difference. Giving through this page is simple, fast, and secure, and it’s the most effective way to support our team’s efforts to improve the lives of those living with scleroderma.

To make a donation, simply click “Donate” and complete the form. Every gift, no matter the size, directly supports the National Scleroderma Foundation’s mission to advance medical research, promote disease awareness, and provide support and education to people with scleroderma, their families, and support networks.

Want to get more involved? Click “Join Us” to sign up and help us raise funds and awareness together!

Our team deeply appreciates your generosity and encouragement. Please consider sharing this page with friends and family who may also want to support. 

Together, we can raise awareness, support those living with scleroderma, and bring us one step closer to finding a cure.